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Inflammatory demyelination in a patient with CMT1A.
Vital A, Vital C, Lagueny A, Ferrer X, Ribière-Bachelier C, Latour P, Petry KG. Vital A, et al. Among authors: latour p. Muscle Nerve. 2003 Sep;28(3):373-6. doi: 10.1002/mus.10404. Muscle Nerve. 2003. PMID: 12929199
Molecular diagnosis of Charcot-Marie-Tooth 1A disease and hereditary neuropathy with liability to pressure palsies by quantifying CMT1A-REP sequences: consequences of recombinations at variant sites on chromosomes 17p11.2-12.
Vandenberghe A, Latour P, Chauplannaz G, Chapon F, Pouget J, Dumas R, Laguenay A, Ollagnon E, Bost M, Duthel S, Chazot G, Boucherat M. Vandenberghe A, et al. Among authors: latour p. Clin Chem. 1996 Jul;42(7):1021-5. Clin Chem. 1996. PMID: 8674184
141 results